A randomized controlled trial of recombinant interferon-beta 1a in Guillain-Barre syndrome

J Pritchard, I A Gray, Z R Idrissova, B R F Lecky, I J Sutton, A V Swan, H J Willison, J B Winer, R A C Hughes

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63 Citations (Scopus)

Abstract

The authors recruited 19 nonambulant patients with Guillain- Barree syndrome into a pilot, double- blind, randomized, placebo- controlled safety trial of interferon beta 1a ( IFN beta- 1a) ( Rebif). Participants received IFN beta- 1a or placebo subcutaneously three times weekly, 22 mu g for the first week and then 44 mu g for up to 24 weeks, in addition to IV immunoglobulin ( IVIg). IFN beta did not have any unexpected interaction with IVIg and there was no significant difference in rate of improvement.
Original languageEnglish
Pages (from-to)1282 - 1284
Number of pages3
JournalNeurology
Volume61
Issue number9
Publication statusPublished - 2003

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